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Taclonex Scalp - 54868-6091-0 - (calcipotriene and betamethasone dipropionate)

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Drug Information of Taclonex Scalp

Product NDC: 54868-6091
Proprietary Name: Taclonex Scalp
Non Proprietary Name: calcipotriene and betamethasone dipropionate
Active Ingredient(s): .643; 50    mg/g; ug/g & nbsp;   calcipotriene and betamethasone dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Taclonex Scalp

Product NDC: 54868-6091
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022185
Marketing Category: NDA
Start Marketing Date: 20091210

Package Information of Taclonex Scalp

Package NDC: 54868-6091-0
Package Description: 1 BOTTLE in 1 CARTON (54868-6091-0) > 60 g in 1 BOTTLE

NDC Information of Taclonex Scalp

NDC Code 54868-6091-0
Proprietary Name Taclonex Scalp
Package Description 1 BOTTLE in 1 CARTON (54868-6091-0) > 60 g in 1 BOTTLE
Product NDC 54868-6091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name calcipotriene and betamethasone dipropionate
Dosage Form Name SUSPENSION
Route Name TOPICAL
Start Marketing Date 20091210
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE
Strength Number .643; 50
Strength Unit mg/g; ug/g
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Taclonex Scalp


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